Taiwan FDA registration 5057891ca1e8583576bcb794530d6849
"Dibo" Kabili Mycobacterium tuberculosis antigen rapid identification reagent (unsterilized)
TW: "帝博" 卡必利 結核桿菌群抗原快速鑑定試劑 (未滅菌)
Taiwan·Risk Class 1·TAUNS LABORATORIES, INC·Registered Feb 25, 2013 – Feb 25, 2018CancelledRegistration details
- Analysis ID
- 5057891ca1e8583576bcb794530d6849
- Customs Code
- DHA04401274800
Company information
- Manufacturer
- TAUNS LABORATORIES, INC
- Manufacturer Country
- Japan
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3370 結核桿菌免疫螢光試劑
- Import Information
- import
Dates and status
- Registration Date
- Feb 25, 2013
- Expiry Date
- Feb 25, 2018
- Cancellation Date
- Mar 20, 2013
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Dibo" Kabili Mycobacterium tuberculosis antigen rapid identification reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5057891ca1e8583576bcb794530d6849 and manufactured by TAUNS LABORATORIES, INC. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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